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Maternal age and the prevalence of congenital heart defects in Europe, 1995–2015: A register‐ based study (CROSBI ID 324002)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Mamasoula, Chrysovalanto ; Bigirumurame, Theophile ; Chadwick, Thomas ; Addor, Marie‐Claude ; Cavero‐ Carbonell, Clara ; Dias, Carlos M. ; Echevarría‐ González‐de‐Garibay, Luis‐Javier ; Gatt, Miriam ; Khoshnood, Babak ; Klungsoyr, Kari et al. Maternal age and the prevalence of congenital heart defects in Europe, 1995–2015: A register‐ based study // Birth defects research, 115 (2023), 6; 583-594. doi: 10.1002/bdr2.2152

Podaci o odgovornosti

Mamasoula, Chrysovalanto ; Bigirumurame, Theophile ; Chadwick, Thomas ; Addor, Marie‐Claude ; Cavero‐ Carbonell, Clara ; Dias, Carlos M. ; Echevarría‐ González‐de‐Garibay, Luis‐Javier ; Gatt, Miriam ; Khoshnood, Babak ; Klungsoyr, Kari ; Randall, Kay ; Stoianova, Sylvia ; Haeusler, Martin ; Nelen, Vera ; Neville, Amanda J. ; Perthus, Isabelle ; Pierini, Anna ; Bertaut‐Nativel, Bénédicte ; Rissmann, Anke ; Rouget, Florence ; Schaub, Bruno ; Tucker, David ; Wellesley, Diana ; Zymak‐ Zakutnia, Natalya ; Barisic, Ingeborg ; de Walle, Hermien E.K. ; Lanzoni, Monica ; Sayers, Gerardine ; Mullaney, Carmel ; Pennington, Lindsay ; Rankin, Judith

engleski

Maternal age and the prevalence of congenital heart defects in Europe, 1995–2015: A register‐ based study

Background: Evidence on the direction and strength of association between maternal age and the prevalence of congenital heart defects (CHD) in different age group categories is conflicting. Some studies have illustrated different trends with an increase in prevalence in younger and older age groups while other studies have reported a linear relationship. Given the increase in maternal age over recent years, it is important to study the CHD prevalence by maternal age. Objectives: To examine the association between maternal age and the prevalence of CHD in Europe between 1995 and 2015 using population-based data from 24 registries belonging to the European Surveillance of Congenital Anomalies (EUROCAT) network. Methods: Associations over time of all nonsyndromic CHD according to maternal age category and for three CHD severity groupings (severity group I: very severe ; severity group II: severe ; severity group III: less severe) were examined using Bayesian multilevel Poisson regression modeling. Further subgroup analyses were undertaken within four maternal age-bands: ≤24, 25-29, 30-34 and 35-44 years. Descriptive summaries are also presented. Results: There were 51, 608 nonsyndromic CHD cases in Europe over the 20-year study period. Total prevalence for all CHD combined was increased for younger mothers (≤24 years) and for mothers 35-44 years of age when compared with mothers aged 25-29 years (reference group) (IRR: 1.05, 95% CI: 1.02, 1.07). The total prevalence was increased for severity group I (very severe) only for younger mothers compared to those aged 25-29 years (IRR: 1.14, 95% CI: 1.04, 1.23). We found an increased prevalence of the following CHD subtypes: double outlet right ventricle (IRR:1.33, 95% CI: 1.09, 1.60), hypoplastic left heart syndrome (IRR: 1.18, 95% CI: 1.05, 1.32), hypoplastic right heart syndrome (IRR: 1.41, 95% CI: 1.05, 1.84), atrioventricular septal defect (IRR: 1.15, 95% CI: 1.01, 1.32), coarctation of aorta (IRR: 1.15, 95% CI: 1.03, 1.28) and atrial septal defect (IRR: 1.08, 95% CI: 1.02, 1.13). For older mothers (35- 44 years) compared to the reference category, we observed an increased risk in the prevalence for severity group II (IRR: 1.09, 95% CI: 1.03, 1.14), severity group III (IRR: 1.05, 95% CI: 1.01, 1.08) and an increased prevalence of the CHD subtypes: Pulmonary valve stenosis (IRR: 1.22, 95% CI: 1.09, 1.34), ASD (IRR: 1.07, 95% CI: 1.02, 1.13), CoA (IRR: 1.18, 95% CI: 1.06, 1.32) and Tetralogy of Fallot (IRR: 1.14, 95% CI: 1.01, 1.28). Finally, for all age categories compared to the reference category, different associations of ASD and an increased prevalence of CoA was also observed. Conclusions: Based on data for cases of CHD from 24 European population-based registries, evidence of a positive association between maternal age and the total prevalence of CHD for younger (≤24 years old) and older (35-44 years old) mothers was observed. The results suggest that young maternal age (≤24 years old) is a factor associated with severe CHD phenotypes while a positive association between advanced maternal age (35-44 years old) and mild CHD phenotypes was observed.

European Surveillance of Congenital Anomalies ; congenital Heart Defects ; maternal age ; prevalence ; register-based study.

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Podaci o izdanju

115 (6)

2023.

583-594

objavljeno

2472-1727

10.1002/bdr2.2152

Povezanost rada

Biotehnologija u biomedicini (prirodno područje, biomedicina i zdravstvo, biotehničko područje)

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